Canonical Allele Identifier: CA2805667690
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4797864_4797865insGGATGGTGAGGAACGCCACAGACAGAGCCACCCT , CM000678.2:g.4797864_4797865insGGATGGTGAGGAACGCCACAGACAGAGCCACCCT GRCh38
NC_000016.9:g.4847865_4847866insGGATGGTGAGGAACGCCACAGACAGAGCCACCCT , CM000678.1:g.4847865_4847866insGGATGGTGAGGAACGCCACAGACAGAGCCACCCT GRCh37
NC_000016.8:g.4787866_4787867insGGATGGTGAGGAACGCCACAGACAGAGCCACCCT NCBI36
NG_032174.1:g.10086_10087insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC , LRG_455:g.10086_10087insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC MANE Select ENSP00000322832.6:n.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000322048.11:c.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000322832.5:n.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000586153.1:c.342-29_342-28insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000464699.1:n.342-29_342-28insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000586336.5:n.795-25_795-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
ENST00000586504.5:c.426-25_426-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
ENST00000587377.5:c.*16-25_*16-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000468343.1:n.*16-25_*16-24insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000587711.5:c.381-25_381-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000467459.1:n.381-25_381-24insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000587843.5:c.*434-25_*434-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000465970.1:n.*434-25_*434-24insAGGGTGGCTCTGTCTGTGGCGTT...
ENST00000588201.5:c.*687-25_*687-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000466529.1:n.*687-25_*687-24insAGGGTGGCTCTGTCTGTGGCGTT...
ENST00000589543.5:n.653-25_653-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
ENST00000591292.5:n.2025-25_2025-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
ENST00000591392.5:c.624-25_624-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC ENSP00000467509.1:n.624-25_624-24insAGGGTGGCTCTGTCTGTGGCGTTCC...
ENST00000592019.1:c.77-50_77-49insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
NM_024589.2:c.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC , LRG_455t1:c.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC NP_078865.1:n.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCA...
NR_046480.1:n.1020-25_1020-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC
XM_006720947.2:c.696-4_696-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC XP_006721010.1:n.696-4_696-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACC...
XM_006720948.2:c.426-4_426-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC XP_006721011.1:n.426-4_426-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACC...
XM_006720947.4:c.696-4_696-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC XP_006721010.1:n.696-4_696-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACC...
XM_006720948.4:c.426-4_426-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC XP_006721011.1:n.426-4_426-3insAGGGTGGCTCTGTCTGTGGCGTTCCTCACC...
NM_024589.3:c.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC MANE Select NP_078865.1:n.696-25_696-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCA...
NR_046480.2:n.703-25_703-24insAGGGTGGCTCTGTCTGTGGCGTTCCTCACCATCC